Canonical Allele Identifier: CA2396214218

Gene: ZDHHC8

Linked Data

• dbSNP Id: rs1602570229
• gnomAD v4: 22-20139683-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139683T>C , CM000684.2:g.20139683T>C	GRCh38
NC_000022.10:g.20127206T>C , CM000684.1:g.20127206T>C	GRCh37
NC_000022.9:g.18507206T>C	NCBI36
NG_021420.1:g.12843T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.385-37T>C MANE Select	ENSP00000334490.7:n.385-37T>C
ENST00000320602.11:c.384+48T>C	ENSP00000317804.7:n.384+48T>C
ENST00000334554.11:c.385-37T>C	ENSP00000334490.7:n.385-37T>C
ENST00000405930.3:c.385-37T>C	ENSP00000384716.3:n.385-37T>C
ENST00000436518.5:c.352-37T>C	ENSP00000412807.1:n.352-37T>C
ENST00000468112.5:n.58-934T>C
NM_001185024.1:c.385-37T>C	NP_001171953.1:n.385-37T>C
NM_013373.3:c.385-37T>C	NP_037505.1:n.385-37T>C
XM_006724239.2:c.385-37T>C	XP_006724302.1:n.385-37T>C
NM_001185024.2:c.385-37T>C	NP_001171953.1:n.385-37T>C
NM_013373.4:c.385-37T>C MANE Select	NP_037505.1:n.385-37T>C